Building assembly including a weather resistant barrier, a sheet for use as a weather resistant barrier, a liquid coating composition and methods of making the foregoing

ABSTRACT

A weather resistive barrier (WRB) for the exterior protection of building substrates can have a water vapor permeability that decreases with increasing temperature. In an embodiment, the WRB includes a coating comprising a LCST polymer, and may further include a second polymer. The WRB can be part of a building assembly, part of a sheet, or a sheet itself, the sheet having an air permeability of less than 0.02 L/(s m2) at a pressure of 75 Pa. Furthermore a liquid coating composition can include a LCST polymer and a second polymer, wherein the liquid coating composition can be adapted that a solid coating formed by the liquid coating composition has an air permeability of less than 0.02 L/(s m2) at a pressure of 75 Pa and a water vapor permeability that decreases with increasing temperature.

CROSS-REFERENCE TO RELATED APPLICATION(S)

This application claims priority under 35 U.S.C. § 120 to and is acontinuation of U.S. application Ser. No. 15/392,716, entitled “BUILDINGASSEMBLY INCLUDING A WEATHER RESISTANT BARRIER, A SHEET FOR USE AS AWEATHER RESISTANT BARRIER, A LIQUID COATING COMPOSITION AND METHODS OFMAKING THE FOREGOING,” by Jeffrey H. PEET et al., filed Dec. 28, 2016,which in turn claims priority under 35 U.S.C. § 119(e) to U.S.Provisional Patent Application No. 62/273,639, entitled “BUILDINGASSEMBLY INCLUDING A WEATHER RESISTANT BARRIER, A SHEET FOR USE AS AWEATHER RESISTANT BARRIER, A LIQUID COATING COMPOSITION AND METHODS OFMAKING THE FOREGOING,” by Jeffrey H. PEET et al., filed Dec. 31, 2015,of which all applications are assigned to the current assignee hereofand incorporated herein by reference in their entireties.

FIELD OF THE DISCLOSURE

The present disclosure relates to a weather resistive barrier (WRB) forbuilding assemblies, sheets for use as weather resistant barriers,liquid coating compositions and methods of making the foregoing.

BACKGROUND

For the construction of wall assemblies, the moisture levels within thewall cavity can be controlled to avoid the formation of mold, which canlead to structural damage and health consequences. An interior smartvapor barrier can be placed on the inner side of an exterior wall cavityto control moisture vapor transmission between the air in the house andthe air in the wall cavity. This type of vapor barrier is often called asmart barrier, because it has an increased moisture vapor permeabilitywith increased humidity: during the winter and heating season, when therelative humidity within the wall cavity is low, the interior barriercan maintain the low moisture levels within the wall cavity, whileduring summer, in the cooling season, when the relative humidity withinthe wall cavity is high, the smart barrier allows the moisture to escapeinto the house.

The above-described interior barrier layer is however not suitable as anexterior barrier layer facing the outdoor environment, because differentmoisture and temperature conditions apply on the exterior surface of awall. There is a need for further improving exterior weather resistantbarriers.

SUMMARY

According to one embodiment, a building assembly comprising a buildingsubstrate and a WRB, the WRB having a water vapor permeability thatdecreases with increasing temperature in a temperature range from 5° C.to 60° C. at a 75% relative humidity (RH).

According to another embodiment, a sheet for use as a WRB comprising acoating, wherein the coating comprises a LCST polymer and a secondpolymer; the sheet has an air permeability of less than 0.02 L/(s m²) ata pressure of 75 Pa; and a water vapor permeability of the sheetdecreases with increasing temperature in a temperature range from 5° C.to 60° C. at 75% RH.

According to a further embodiment, a liquid coating compositioncomprising a LCST polymer and a second polymer, wherein the liquidcoating composition is adapted that a solid coating formed by the liquidcoating composition has an air permeability of less than 0.02 L/(s m²)at a pressure of 75 Pa; and a water vapor permeability of the solidcoating decreases with increasing temperature in a temperature rangefrom 5° C. to 60° C. at 75% RH.

BRIEF DESCRIPTION OF THE DRAWINGS

The present disclosure may be better understood, and its numerousfeatures and advantages made apparent to those skilled in the art byreferencing to the accompanying drawings.

FIG. 1 includes an illustration of a temperature dependentconformational change of a LCST polymer below LCST and above LCST.

FIG. 2 includes an illustration of a WRB in form of a one-layer coatingapplied on a building substrate according to one embodiment.

FIG. 3 is a graph showing the water vapor permeability of threedifferent LCST polymer coatings (100 wt % LCST polymer in the drycoating) at varying temperature and 75% RH according to certainembodiments.

FIG. 4 is a graph showing the water vapor permeability of two differentLCST polymer coatings (100 wt % LCST polymer in the dry coating) at 25%RH and 75% RH and varying temperature according to certain embodiments.

FIG. 5 is a graph showing the water vapor permeability of two differentLCST polymer coatings, wherein the LCST polymer is distributed in apolymeric matrix (23 wt % LCST polymer in the dry coating) at varyingtemperature and 75% RH according to certain embodiments.

DETAILED DESCRIPTION

As used herein, the terms “comprises,” “comprising,” “includes,”“including,” “has,” “having” or any other variation thereof, areintended to cover a non-exclusive inclusion. For example, a process,method, article, or apparatus that comprises a list of features is notnecessarily limited only to those features but may include otherfeatures not expressly listed or inherent to such process, method,article, or apparatus.

As used herein, and unless expressly stated to the contrary, “or” refersto an inclusive-or and not to an exclusive-or. For example, a conditionA or B is satisfied by any one of the following: A is true (or present)and B is false (or not present), A is false (or not present) and B istrue (or present), and both A and B are true (or present).

Also, the use of “a” or “an” are employed to describe elements andcomponents described herein. This is done merely for convenience and togive a general sense of the scope of the invention. This descriptionshould be read to include one or at least one and the singular alsoincludes the plural unless it is obvious that it is meant otherwise.

Various embodiments of the present disclosure will now be described, byway of example only, with reference to the accompanying drawings.

The present disclosure relates to a WRB that can be applied in form of acoating on a building substrate for exterior weather protection and canregulate water vapor permeation such that the water vapor permeabilitydecreases with increasing temperature.

In embodiments, the coating of the WRB can include a lower criticalsolution (LCST) polymer and may further include a second polymer. Asused herein, the terms “a LCST polymer” and “a second polymer” meansboth, the singular form and the plural form, such as one or more LCSTpolymers and one or more second polymers.

As used herein, the term LCST polymer is intended to mean athermoresponsive polymer which can undergo a change of itsthree-dimensional structure at a certain temperature, also called theLCST. In the present specification, the terms LCST polymer andthermoresponsive polymer are used interchangeable.

LCST behavior of thermoresponsive polymers can be observed in solution:below the LCST, a thermoresponsive polymer is fully miscible in asolution, but at a certain temperature (the LCST) the polymer begins tocollapse and becomes insoluble. Polymers which are known to have LCSTbehavior in solution are not well investigated in the solid phase withregard to this thermoresponsive property. Not being bound to theory, itis speculated that a conformational change of the LCST polymerdistributed within a solid matrix, such as a solid coating, can beassociated with changes of the porous structure and the hydrophiliccharacter of the solid matrix and thereby can cause a change in watervapor permeability. As demonstrated in FIG. 1, it is assumed that a LCSTpolymer distributed within a polymeric matrix undergoes a conformationalchange at its LCST, such that above the LCST, a more dense structure isformed which causes a decrease in water vapor permeability compared to awater vapor permeability at a temperature below the LCST.

As used herein, all water vapor permeability values have the unit USperm, wherein 1 US perm converts to 0.659045 metric perms (m.p.).

As used herein, the term coating is intended to mean a single coatinglayer or a multi-layer coating that has been applied to a substrate witha liquid coating composition after drying. In embodiments, the termcoating may also relate to a thin sheet or film, for example, anextruded film comprising the LCST polymer distributed within a polymericmatrix.

As used herein, the term polymeric matrix is intended to mean apolymeric network formed by a second polymer different from the LCSTpolymer. The LCST polymer can be distributed within the polymeric matrixof the second polymer. In the present disclosure, the term polymericmatrix is interchangeable used with the term “second polymer” or “matrixpolymer.”

In one embodiment, the LCST polymer can be mixed with the second polymerwithout forming a chemical bonding. In particular embodiments, each ofthe LSCT polymer and the second polymer may be a homopolymer, part of acopolymer or could be a combination of polymers. In another embodiment,the LCST polymer can by grafted via chemical bondings on the secondpolymer of the polymeric matrix.

In embodiments, the LCST polymer contained in the WRB coating of thepresent disclosure can be a hydroxyalkyl cellulose, apoly(alkylacrylamide), a poly(vinyl methyl ether), a polyetheramine, apolyether; an alkylgycidylether; a polyphosphester; or any combinationthereof.

In particular embodiments, the LCST polymer of the WRB coating of thepresent disclosure can include hydroxypropylcellulose,poly(N-isopropylacrylamide), poly(N-(tert-butyl)acrylamide), a monoamineof a poly(ethylene propylene) copolymer (for example, JeffamineM-2005™-brand polymer available from Huntsman Corporation, TheWoodlands, Tex., USA), or any combination thereof.

Other non-limiting examples of LCST-polymers that may be suitable forthe WRB coating of the present disclosure can be N-substitutedpoly(acrylamide); poly(methacrylamide) (PMAAm); poly(N-ethylacrylamide)(PEAAm); poly(N-ethylmethacrylamide) (PEMAAm);poly(N,N-ethylmethylacrylamide); poly(N,N-diethylacrylamide) (PDEAAm);poly(N-n-propylacrylamide) (PnPAAm); poly(N-n-propylmethacrylamide)(PnPMAAm); poly(N-isopropylacrylamide) (PNIPAM);poly(N-isopropylmethacrylamide) (PNIPMAm); poly(N-cyclopropylacrylamide)(PcPAAm); poly(N-(L)-(1-hydroxymethyl)propylmethacrylamide)(P(L-HMPMAAm)); poly(N-acryloylpyrrolidine); poly(N-acryloylpiperidine)(PAOPip); poly(N-vinyl caprolactam) (PVCL); poly(N-vinylpropylacetamide); poly(N-vinyl-5-methyl-2-oxazolidone); poly(N-vinylisobutyramide) (PViBAm); poly(methyl 2-alkylamidoacrylate); poly(methyl2-propionamidoacrylate); poly(methyl 2-isobutyracrylate);poly(2-substituted-2-oxazoline); poly(2-ethyl-2-oxazoline) (PEOz);poly(2-n-propyl-2-oxazoline) (PnPOz); poly(2-isopropyl-2-oxazoline)(PiPOz); poly(ethyleneoxide) (PEO); poly(ethylene glycol) (PEG)poly(propyleneoxide) (PPO); poly(propylene glycol) PPG; poly(vinylether)(PVEth); poly(methylvinylether) (PMVEth); poly(2-methoxyethylvinylether)(PMOVEth); poly(2-ethoxyethylvinylether) (PEOVEth);poly(2-(2-ethoxy)ethoxyethylvinylether); poly(4-hydroxybutylvinylether);poly(methyl glycidyl ether); poly(ethyl glycidyl ether);poly(ethoxyethyl glycidyl ether);poly(2-ethoxy-2-oxo-1,3,2-dioxaphospholane); poly(ethyl ethylenehosphate); poly(2-isopropoxy-2-oxo-1,3,2-dioxaphospholane);poly(isopropyl ethylene phosphate); poly(N-methylacrylamide) (PMAAm);poly(N,N-dimethylacrylamide) (PDMAAm); poly(N-alkyl(meth)acrylamide)bearing hydroxyl groups; poly(N-ethylmethacrylamide) (PNEMAAm);poly(N,N-ethylmethylacrylamide) (PNNEMAAm); poly(N-n-propylacrylamide)(PnPAAm); poly(N-isopropylacrylamide) (PiPAAm);poly(N-vinylisobutyramide) (PViBAm); poly(-n-propyl-2-oxazoline)(PnPOz); poly(-isopropyl-2-oxazoline) (PiPOz); polyleucine (PLeu);poly(vinylpyrrolidone) (PVP); poly(N-acryloylmorpholine) (pAOM);poly(N-tert-butylacrylamide); poly(-substituted-2-oxazoline);poly(vinylalcohol) (PVA); poly(vinylacetate) (PVAc);poly(propyleneoxide) (PPO); poly[2-(2-ethoxyethoxy)ethylacrylate](PEEO2A); poly[2-(2-methoxyethoxy)ethylmethacrylate)] (PMEO2MA);poly(2-[2-(2-methoxyethoxy)ethoxy]ethylmethacrylate) (PMEO3MA);poly[oligo(ethyleneglycol)methacrylate] (POEGMA) with side chains ofeight or nine ethylene oxide units; poly(-hydroxypropylacrylate) (PHPA);poly(2-hydroxyethylmethacrylate) (PHEMA); N-substitutedpolymethacrylamides with alkylaldonamide side chains;poly(amidohydroxyurethane) (PAmHU); 1,4-butanediol diglycidyl ether withtriols, such as trimethylolethane and trimethylolpropane;1,2,7,8-diepoxyoctane with ethylene glycol, di(ethylene glycol),tri(ethylene glycol), 1,2-propanediol, and glycerol; oligo(ethyleneoxide)-grafted polylactides; methoxy-terminated dendronizedpolymethacrylates; isobutyramide-terminated poly(amidoamine) dendrimers;poly(organophosphazene with two side groups of poly(ethylene oxide) andamino acid esters; poly[6-(acryloyloxymethyl)uracil];poly(methylvinylether) (PMVEth); poly(methacrylamide) (PMAAm);poly(N-acrylylglycinamide); and poly(N-methacrylylglycinamide). Afurther group of LCST polymers may be protein-based LCST polymers, suchas of the structure (Poly(VPGXG), wherein V is L-valine, P is L-proline,G is glycine, and X is any natural amino acid except proline);Poly(L-proline) (PPro); Poly(N-acryloyl-L-proline methyl ester)(PAProMEs); and Poly(N-acryloyl-4-trans-hydroxy-L-proline methyl ester)(PAHProMEs).

It should be noted that not all polymers falling under the abovementioned polymer classes are LCST polymers, i.e., polymers having theabove-described thermoresponsive behavior in solution. To identify aspecific compound as a LCST polymer, if not already known fromliterature publications, its LCST behavior can be confirmed by apractical experiment with defined system parameters, and is difficult topredict. A suitable experiment to investigate a potential LCST propertyof a polymer is the cloud point measurement, the temperature at which asoluble compound starts coagulating in a solution and makes the solutioncloudy, as also in more detail described in the experimental part of thepresent disclosure.

An LCST polymer which shows thermoresponsive behavior in solution may ormay not have the same thermoresponsive behavior if distributed within asolid polymeric matrix, such as a dried coating. Not to be bound totheory, thermoresponsive behavior within a solid coating may depend onseveral factors. Non-limiting examples of such factors may be the typeof polymeric matrix (second polymer) wherein the LCST polymer isdistributed, the amount of LCST polymer in the coating, the thickness ofthe coating, the density of the coating, the humidity, or anycombination of these factors.

In embodiments, the polymeric matrix in which the LCST polymer can bedistributed may include an acrylic polymer, an acrylic copolymer, astyrene acrylic copolymer, a vinyl acetate polymer, a vinyl acetateethylene copolymer, an olefin wax, a polyethylene, a polypropylene, apolyurethane, a polyester, a vinylidene chloride polymer, astyrene-butadiene copolymer an acrylonitrile-butadiene copolymer, or anycombination thereof. In another particular aspect, the second polymercan be also a LCST polymer.

In certain embodiments, an amount of the LCST polymer in the WRB coatingcan be at least 0.5 wt %, such as at least 1 wt %, at least 5 wt %, atleast 10 wt %, or at least 20 wt % based on the total weight of thecoating. In other embodiments, the amount of LCST polymer in the coatingmay be not greater than 99 wt %, such as not greater than 90 wt %, notgreater than 80 wt %, or not greater than 50 wt % based on the totalweight of the coating. It will be appreciated that the amount of LCSTpolymer in the coating can be a value within any of the maximum andminimum values noted above, such as from 0.5 wt % to 99 wt %, from 3 wt% to 85 wt %, or from 15 wt % to 50 wt % based on the total weight ofthe coating.

The second polymer of the coating can be included in an amount of atleast 1.0 wt % based on the total weight of the coating, such as atleast 10 wt %, at least 20 wt %, at least 30 wt %, or at least 40 wt %.In other embodiments, the amount of the second polymer in the coatingmay be not greater than 99 wt %, such as not greater than 95 wt %, notgreater than 90 wt %, not greater than 85 wt %, or not greater than 80wt % based on the total weight of the coating. It will be appreciatedthat the amount of LCST polymer in the coating can be a value within anyof the maximum and minimum values noted above, such as from 1.0 wt % to99 wt %, from 5 wt % to 95 wt %, or from 35 wt % to 90 wt % based on thetotal weight of the coating.

In other embodiments, the coating of the WRB can further include atleast one of an UV absorber, a filler, a dye, an anti-foaming agent, aviscosity modifier, a dispersant, a surfactant, or any combinationthereof.

In certain embodiments, the WRB coating of the present disclosure canhave a thickness of at least 10 μm, such as at least 20 μm, at least 50μm, or at least 100 μm. In yet other embodiments the coating can have athickness of not greater than 800 μm, such as not greater than 700 μm,not greater than 600 μm, or not greater than 500 μm. It will beappreciated that the thickness of the coating can be a value within anyof the maximum and minimum values noted above, such as from 10 μm to 800μm, from 15 μm to 650 μm, or from 20 μm to 550 μm.

The WRB of the present disclosure can be suitable for the exteriorweather protection of a building substrate and can have the desiredadvantage that it regulates the water vapor flow, such that water vaporpermeability decreases with increasing temperature in a temperaturerange of 5° C. to 85° C., particularly within a temperature range from5° C. to 60° C. In certain embodiments, the water vapor permeability ofthe WRB coating of the present disclosure can have a decrease of atleast 50% as temperature increases from 5° C. to 60° C. In otherembodiments, the water vapor permeability may decrease by at least 55%,such as 60%, 70%, 80%, or 90% at a temperature increase from 5° C. to60° C.

The decrease in water vapor permeability of a WRB coating may not becontinuous over the whole temperature range, but can also occur as acertain drop in permeability, specifically close to the cloud pointtemperature of the LCST polymer.

In particular embodiments, the water vapor permeability of the coatingat a temperature of 25° C. or below can be at least 10 US perms, such asat least 15 US perms, at least 20 US perms, at least 30 US perms, atleast 50 US perms, or at least 100 US perms. In yet other embodiments,the water vapor permeability at a temperature of 45° C. or higher maynot be greater than 5 US perms, such as not greater than 4 US perms, notgreater than 3 US perms, not greater than 2 US perms, or not greaterthan 1 US perm.

The water vapor permeability of the WRB of the present disclosure canfurther depend on the relative humidity of its surrounding. It has beensurprisingly observed that a thermoresponsive behavior of the WRBcoatings can occur at high humidity, such as 75% RH or 95% RH, but notnecessarily also at low humidity, such as at 25% RH. Not wishing to bebound to theory, it appears that the presence of water allows an easierconformational change of the LCST polymer in the polymeric matrix bymaking the matrix more hydrophilic.

The WRB coating of the present disclosure can be attached to or coatedonto a building substrate to form a building assembly. As used herein,the term building substrate can be any structure suitable for theconstruction of buildings that would benefit from a controlled watervapor flow, specifically where it is desired having a decrease in watervapor permeability with increasing relative humidity. Non-limitingexamples for building substrates can be, for example, a wall assembly, aboard, a siding, a sheet good, or a panel. In a particular embodiment,the building substrate may be a board comprising gypsum.

In one embodiment, the WRB of the present disclosure can be aone-layer-coating in direct contact with at least one outer surface of abuilding substrate, see FIG. 2.

The present disclosure is also related to a sheet for use as a WRB. Inembodiments, the sheet can be a composite of a porous substrate and theabove-described coating, wherein the coating may overlie at least afirst surface of the porous substrate. In particular embodiments, anadhesive layer may overlie a second opposite surface of the poroussubstrate and a removable liner may be attached to the adhesive layer ofthe sheet. In a particular embodiment, the sheet can be a self-adheredsheet for the exterior protection of a building substrate. In anotherparticular embodiment, the sheet of the present disclosure may be formedby the coating only, for example, in form of a thin extruded film.

In embodiments, the sheet of the present disclosure can have an airpermeability of less than 0.02 L/(s m²) at a pressure of 75 Pa. As usedherein, when referring to the air permeability, all cited airpermeability values are obtained under the testing procedure as setforth in ASTM E2178 (2013).

The present disclosure is further related to a liquid coatingcomposition suitable for making the above-described coating of the WRB.In embodiments, the liquid coating composition can include at least afirst polymer and a second polymer, whereby the first polymer caninclude an LCST polymer. The liquid coating composition can be adaptedthat a solid coating formed by the liquid coating composition has an airpermeability of greater than 0.02 L/(s m²) at a pressure of 75 Pa.

The LCST polymer and the second polymer may be selected as describedabove with regard to the WRB coatings.

In embodiments, the liquid coating composition can comprise water in anamount of at least 5 wt %, such as at least 10 wt %, at least 15 wt %,or at least 20 wt % based on a total weight of the liquid coatingcomposition. In other embodiments, the amount of water in the liquidcoating composition may be not greater than 95 wt %, such as not greaterthan 90 wt %, not greater than 80 wt %, or not greater than 70 wt %. Itwill be appreciated that the water content of the liquid coatingcomposition can be a value within any of the maximum and minimum valuesnoted above, such as from 5 wt % to 95 wt %, from 20 wt % to 85 wt %, orfrom 25 wt % to 75 wt %.

In other embodiments, the liquid coating composition may contain asolvent different then water, or a mixture of water and another solvent.

In embodiments, the liquid coating composition of the present disclosurecan further optionally include at least one of an UV absorber, a filler,a dye, an anti-foaming agent, a viscosity modifier, a dispersant, asurfactant, or any combination thereof.

In certain embodiments, the filler of the liquid coating composition maycomprise inorganic materials, organic materials or combinations thereof.Specific fillers can include a clay, a montmorillonite, calciumcarbonate, barium sulfate, a bentonite, a muscovite, an illite, acookeite, a kaolonite, a chlorite, gypsum, silica, talc, carbon black,diatomaceous earth, alumina, titania, or combinations thereof. In someembodiments, the filler may provide reinforcement in the cured coating,may provide flame retardancy in the cured coating, or may improve thephysical properties of the cured coating (e.g., decrease the coefficientof linear thermal expansion (CLTE) as compared to the CLTE of a curedcomposition without the filler). In certain embodiments, the filler canbe present in the liquid coating composition in a range of from 0 wt %to 30 wt %, based on the total weight of the liquid coating composition.

In certain examples, the liquid coating compositions can include one ormore biocidal agents. The biocidal agent can be effective to deter orprevent growth of organisms on the coating and/or surface of thebuilding substrate. In some embodiments, the biocidal agent can beeffective as a fungicide, e.g., a moldicide, to prevent growth of moldor other fungus on the surface of the substrate. In other embodiments,the biocidal agent can be effective to prevent growth of bacteria, moss,algae or other organisms on the surface of the substrate. Where present,the biocidal agent may be present in an effective amount to deter orprevent growth of bio organisms.

The liquid coating composition can also have a desirable viscosity. Forexample, in particular embodiments, the composition can have a viscosityof at least about 1000 cps at a shear rate of 1 s⁻¹ at a temperature of21° C. In further embodiments, the composition can have a viscosity ofno greater than about 1000 cps at a shear rate of 1000 s⁻¹ at atemperature of 21° C. Moreover, the composition can have a viscosity ofat least about 5000 cps at a shear rate of 1 s⁻¹ at a temperature of 21°C. and a viscosity of not greater than about 1000 cps at a shear rate of1000 s⁻¹ at a temperature of 21° C.

The liquid coating composition can also be described by properties aftercuring. As used herein, the cured liquid coating composition is referredto the coating and can be a major part of WRB or can establish thecomplete WRB of the present disclosure. In particular embodiments, thecoating can have a particular coat weight. For example, the coating canhave a coat weight of at least about 10 g/m², at least about 20 g/m², oreven at least about 40 g/m². In further embodiments, the coating canhave a coat weight of not greater than about 120 g/m². It will beappreciated that the coat weight can have a value within a range of anyof the maximum and minimum values provided above, such as from about 10g/m² to about 120 g/m², or from about 40 g/m² to about 100 g/m².

The present disclosure is further directed to a method for making theabove-described WRB or building assembly.

In particular embodiments, the method can include providing a buildingsubstrate, and applying the above-described liquid coating compositionon at least one outer surface of the building substrate. The liquidcoating composition can be applied onto the building substrate, forexample, by spraying, dip-coating, or coating via a Mayer rod, a brushor a blade. The applied liquid coating composition can be air dried,infrared radiation dried, or dried at elevated temperatures up to 85° C.

As demonstrated in the examples described below, it was possible todevelop and produce solid barrier coatings including LCST polymers,wherein the coatings have the desired characteristic of a decrease inwater vapor permeability with increasing temperature. Such behaviormakes the coatings of the present disclosure suitable for use inexterior weather resistive barriers (WRB) for building assemblies. Inwinter, when the temperature and relative humidity within the wallcavity are high compared to the cold and dry outdoor air, the membranecan be permeable and allow moisture vapor to escape the wall cavity,while in summer, when the temperature and relative humidity levelswithin the wall cavity are low compared to the hot and humid outsideenvironment, the membrane can act as a barrier and not allow the outdoormoisture to penetrate within the wall.

Many different aspects and embodiments are possible. Some of thoseaspects and embodiments are described herein. After reading thisspecification, skilled artisans will appreciate that those aspects andembodiments are only illustrative and do not limit the scope of thepresent invention. Embodiments may be in accordance with any one or moreof the embodiments as listed below.

EMBODIMENTS Embodiment 1

A building assembly comprising a building substrate and a weatherresistive barrier (WRB), the WRB having a water vapor permeability thatdecreases with increasing temperature in a temperature range from 5° C.to 60° C. at 75% relative humidity (RH).

Embodiment 2

The building assembly of embodiment 1, wherein the WRB comprises acoating including a lower critical solution temperature (LCST) polymer.

Embodiment 3

The building assembly of embodiment 2, wherein the coating furthercomprises a second polymer different from the LCST polymer.

Embodiment 4

The building assembly or claim 1, wherein the WRB comprises a coatingincluding a lower critical solution temperature (LCST) polymer and asecond polymer different from the LCST polymer.

Embodiment 5

The building assembly of any of embodiments 2, 3, or 4, wherein the LCSTpolymer includes a hydroxyalkyl cellulose, a poly(alkylacrylamide), apoly(vinyl methyl ether), a polyetheramine, or any combination thereof.

Embodiment 6

The building assembly of embodiment 5, wherein the LCST polymer includesa hydroxypropylcellulose, Poly(N-isopropylacrylamide),poly(N-(tert-butyl)acrylamide), a monoamine of a poly(ethylenepropylene) copolymer, or any combination thereof.

Embodiment 7

The building assembly of any of embodiments 2 to 6, wherein an amount ofthe LCST polymer in the coating is at least 0.5 wt % based on the totalweight of the coating.

Embodiment 8

The building assembly of any of embodiments 3 to 7, wherein the secondpolymer includes an acrylic polymer, an acrylic copolymer, a styreneacrylic copolymer, a vinyl acetate polymer, a vinyl acetate ethylenecopolymer, an olefin wax, a polyethylene, a polypropylene, apolyurethane, a polyester, a vinylidene chloride polymer, astyrene-butadiene copolymer an acrylonitrile-butadiene copolymer, or anycombination thereof.

Embodiment 9

The building assembly of any of the preceding embodiments, wherein theWRB further comprises at least one of an UV absorber, a filler, a dye,an anti-foaming agent, a viscosity modifier, a dispersant, a surfactant,or any combination thereof.

Embodiment 10

The building assembly of any of the preceding embodiments, wherein thecoating of the WRB has a thickness of at least 10 μm and not greaterthan 500 μm.

Embodiment 11

The building assembly of any of the preceding embodiments, wherein theWRB has a water vapor permeability of not greater than 5 US perms, suchas not greater than 3 US perms, or not greater than 1 US perm at atemperature of at least 45° C.

Embodiment 12

The building assembly of any of the preceding embodiments, wherein theWRB has a water vapor permeability of at least 10 US perms, such as atleast at least 15 US perms, at least 20 US perms, or at least 30 USperms at a temperature of less than 25° C.

Embodiment 13

The building assembly of any of embodiments 2 to 12, wherein the coatingis a one-layer-coating and the coating is in direct contact with atleast one outer surface of the building substrate.

Embodiment 14

The building assembly of any of the preceding embodiments, wherein thebuilding substrate is a board, a panel, or a siding.

Embodiment 15

The building assembly of embodiment 14, wherein the building substrateis a board comprising gypsum.

Embodiment 16

The building assembly of any of the preceding embodiments, wherein thewater vapor permeability of the WRB decreases by at least 50% at atemperature increase from 5° C. to 60° C.

Embodiment 17

The building assembly of any of the precedent embodiments, wherein thewater vapor permeability at a temperature below 25° C. is at least 12 USperms, and the water vapor permeability at a temperature greater than45° C. is not greater than 6 US perms.

Embodiment 18

A sheet for use as a WRB comprising a coating, wherein the coatingcomprises a LCST polymer and a second polymer; the sheet has an airpermeability of less than 0.02 L/(s m²) at a pressure of 75 Pa; and awater vapor permeability of the sheet decreases with increasingtemperature in a temperature range from 5° C. to 60° C. at a relativehumidity of 75% RH.

Embodiment 19

The sheet of embodiment 18, wherein the coating overlies a first surfaceof a porous substrate.

Embodiment 20

The sheet of embodiments 18 or 19, wherein the sheet further comprisesan adhesive layer overlying a second surface of the porous substrate.

Embodiment 21

The sheet of embodiment 20, wherein the sheet comprises a removableliner attached to the adhesive layer.

Embodiment 22

The sheet of any of embodiments 18 to 20, wherein the sheet is anself-adhered sheet.

Embodiment 23

The sheet of embodiment 18, wherein the sheet is an extruded film.

Embodiment 24

The sheet of any of embodiments 18 to 23, wherein the LCST polymercomprises a hydro alkyl cellulose, a poly(alkylacrylamide), a poly(vinylmethyl ether), a polyetheramine, or any combination thereof.

Embodiment 25

The sheet of embodiment 24, wherein the LCST polymer includeshydroxypropylcellulose, poly(N-isopropylacrylamide),poly(N-(tert-butyl)acrylamide), a monoamine of a poly(ethylenepropylene) copolymer, or any combination thereof.

Embodiment 26

The sheet of any of embodiments 18 to 25, wherein the sheet has a watervapor permeability of not greater than 5 US perms, such as not greaterthan 3 US perms, or not greater than 1 US perm at a temperature of atleast 45° C.

Embodiment 27

The sheet of any of embodiments 18 to 25, wherein the sheet has a watervapor permeability of at least 10 US perms, such as at least at least 20US perms, at least 30 US perms, or at least 40 US perms at a temperatureof less than 25° C.

Embodiment 28

The sheet of any of embodiments 18 to 27, wherein the water vaporpermeability of the WRB decreases by at least 50% at a temperatureincrease from 5° C. to 60° C.

Embodiment 29

The sheet of any of embodiments 18 to 25 or 28, wherein the water vaporpermeability at a temperature below 25° C. is at least 12 US perms, andthe water vapor permeability at a temperature greater than 45° C. is notgreater than 6 US perms.

Embodiment 30

A method for making a building component, comprising: providing abuilding substrate; and attaching a WRB to at least one outer surface ofthe building substrate, wherein the WRB comprises a coating including aLCST polymer and a second polymer.

Embodiment 31

The method of embodiment 30, comprising: preparing an aqueous coatingsolution comprising the LCST polymer and the second polymer; applyingthe aqueous coating solution onto at least one outer surface of thebuilding substrate; and drying the aqueous coating solution to form thecoating.

Embodiment 32

The method of embodiments 30 or 31, wherein the building substrate is aboard, panel, or siding.

Embodiment 33

The method of embodiment 32, wherein the building substrate is a boardcomprising gypsum.

Embodiment 34

The method of any of embodiments 30 to 33, wherein the WRB has a watervapor permeability that decreases with increasing temperature in atemperature range of 5° C. to 85° C., such as 5° C. to 75° C., or 5° C.to 60° C.

Embodiment 35

The method of any of embodiments 30 to 34, wherein the WRB has a watervapor permeability not greater than 5 US perms, such as not greater than3 US perms, or not greater than 1 US perm at a temperature of at least45° C.

Embodiment 36

The method of any of embodiments 30 to 35, wherein the WRB has a watervapor permeability of at least 10 US perms, such as at least at least 20US perms, at least 30 US perms, or at least 40 US perms at a temperatureof less than 25° C.

Embodiment 37

A liquid coating composition comprising a first polymer and a secondpolymer, wherein the first polymer comprises a LCST polymer, and whereinthe liquid coating composition is adapted that a solid coating formed bythe liquid coating composition has an air permeability of less than 0.02L/(s m²) at a pressure of 75 Pa, and a water vapor permeability of thesolid coating decreases with increasing temperature in a temperaturerange from 5° C. to 60° C. at a relative humidity of 75% RH.

Embodiment 38

The liquid coating composition of embodiment 37, wherein the coatingcomposition comprises water in an amount of at least 5 wt %.

Embodiment 39

The liquid coating composition of embodiments 37 or 38, wherein the LCSTpolymer includes a hydroxyalkyl cellulose, a poly(alkylacrylamide), apoly(vinyl methyl ether), a polyetheramine, or any combination thereof.

Embodiment 40

The liquid coating composition of embodiment 39, wherein the LCSTpolymer includes hydroxypropylcellulose, poly(N-isopropylacrylamide),poly(N-(tert-butyl)acrylamide), a monoamine of a poly(ethylenepropylene) copolymer, or any combination thereof.

Embodiment 41

The liquid coating composition of any of embodiments 37 to 40, whereinthe second polymer is an emulsion polymer.

Embodiment 42

The liquid coating composition of any of embodiments 37 to 41, whereinthe second polymer includes an acrylic polymer, a acrylic copolymer, astyrene acrylic copolymer, a vinyl acetate polymer, a vinyl acetateethylene copolymer, an olefin wax, a polyurethane, a vinylidene chloridepolymer, a styrene-butadiene copolymer, an acrylonitrile-butadienecopolymer, or any combination thereof.

EXAMPLES

The following non-limiting examples illustrate the concepts as describedherein.

Example 1

The cloud points of two different LCST polymers, hydroxypropyl cellulose(HPC) and Poly(N-isopropylacrylamide) (PNIPAAM), were tested in aqueoussolutions at varying concentrations. The cloud point is related to thetemperature of a thermoresponsive polymer at which the dissolved polymerstarts to coagulate and to separate from the solution, thereby causing acloudiness of the solution. The cloud point can be an indication of theLCST of an investigated thermoresponsive polymer.

The cloud tests were started at an initial temperature of 25° C., andthe temperature of the polymer solutions was slowly increased at a speedof about 2° C. every five minutes. The tests were also conducted in thereverse direction to determine the clearing point at which thecoagulated polymer dissolves again. The decrease in temperature wasregulated also at a speed of 2° C. every five minutes. For the testevaluation, the temperatures at which the clouding and clearing beganwas noted, as well as the temperature at which the solutions were fullyclouded or fully cleared.

A summary of the cloud test results is shown in Table 1 for PNIPAAM andin Table 2 for HPC. It can be seen that PNIPAAM has a cloud point in therange of 31° C. to 33° C., while HPC has a cloud point in the range of46° C. to 48° C. Both materials showed a reversible clouding effect,whereby the temperature of the clearing point was slightly lower thanthe temperature of the clouding point. Different concentrations did notlead to a change in the clouding point temperature.

TABLE 1 Cloud test results of PNIPAAM solutions with varyingconcentrations. Clouding Point Clearing Point (heating of solution)(cooling of solution) Final Final Initial Clouding Initial ClearingPNIPAAM Clouding Point Clearing Point Point Concentration Point [° C.][° C.] [° C.] [° C.] .5%  33.5 35.2 33.5 31.1 1% 33.1 34.3 33.2 32.1 5%33.4 33.7 33 31.1 10%  32.6 33.3 32.9 31.1

TABLE 2 Cloud test results of HPC solutions with varying concentrations.Clouding Point Clearing Point (heating of solution) (cooling ofsolution) Final Final Initial Clouding Initial Clearing HPC CloudingPoint Point Clearing Point Point Concentration [° C.] [° C.] [° C.] [°C.] .5%  49.4 52.6 50.8 47.6 1% 48 57.4 48.6 47.3 5% 46.5 47.9 47.1 46.510%  48.4 48.9 48.3 46

Example 2

Permeability testing of LCST polymer coatings (100% LCST polymer in drycoating) at varying temperature:

Three aqueous liquid coating solutions were prepared, each including oneof the following LCST polymers: 1) poly[2-(2-ethoxyethoxy)ethylacrylate](PEEO2A from Aldrich); 2) polyvinylalcohol (PVA LM25 from Kuraray); and3) a polyurethane made of polypropylene glycol (PPG4000) and isocyanate(Desmodur N75MPA).

The liquid coating solutions were applied via a Mayer rod on an uncoatedbrown Kraft paper (80 g/m²) and allowed to dry. The resulting drycoating thicknesses for all samples were 100 μm, and contained 100 wt %of the LCST polymer based on the total weight of the coating.

The dried samples were analyzed with regard to their water vaporpermeability at 75% RH, at five different temperatures: 10° C.; 20° C.;30° C.; 40° C.; and 50° C.

A summary of the prepared coating samples and the measured water vaporpermeability values can be seen in Table 3 and FIG. 3. For all LCSTpolymer coating layers, a decrease in water vapor permeability withincreasing temperature could be observed over the tested temperaturerange.

TABLE 3 LCST in Thickness dry of dry coating coating Permeability [USPerm] Sample LCST Polymer [%] [μm] 10° C. 20° C. 30° C. 40° C. 50° C. E1PEEO2A 100 100 207.2 162.2 80.15 67.2 E1 PVA LM25 100 100 227.8 142.6128.7 72.3 37.6 E3 Polyurethane of 100 100 177.7 116.4 63.2 45 27.5PG4000 + N75MPA

Example 3

Permeability testing of LCST polymer coatings (100% LCST polymer in drycoating) at varying temperature and at two different humidities:

Coated paper samples have been prepared according to the same procedureas described in Example 2, except that as LCST polymers were usedhydroxypropyl cellulose (HPC) from Fisher Scientific, andPoly(N-isopropylacrylamide) (PNIPAAM) from Sigma Aldrich. Water vaporpermeability were measured at two different humidities, such as 25% RHand 75% RH. For each humidity, two different temperatures were chosenfor the permeability measurements: 20° C. and 60° C. As can be seen inTable 4 and FIG. 4, the PNIPAAM layer showed a decrease in water vaporpermeability at increasing temperature for both humidity conditions, at25% RH and 75% RH. In the case of the HPC layer, a decrease in watervapor permeability was observed at 75% RH, but not at 25% RH.

TABLE 4 Permeability [US Perm] LCST LCST Thickness of dry 25% RH 75% RHSample Polymer [wt %] coating [μm] 20° C. 60° C. 20° C. 60° C. E4 HPC100 31 29.3 40.8 145 111 E5 PNIPAAM 100 31 62.2 35.9 120.4 84.3

Example 4

Permeability testing of coatings with LCST polymer contained in apolymeric matrix: Solid coatings were prepared with LCST polymers HPC orPNIPAAM contained in a polymeric matrix. As matrix polymers (secondpolymer) were used Latex XU31591, a styrene butadiene based polymer(from Trinseo); Latex XU31904, a butadiene-vinylidene chloride basedpolymer (from Trinseo), and Lipacryl MB-364, a full acrylic polymer(from Dow Chemical Company). The coatings varied in the amount of LCSTpolymer, the amount of matrix polymer and the thickness of the drycoatings (see Table 5). Permeability measurements were conducted at 25%RH and 75% RH and at two different temperatures: 20° C. and 60° C.

For HPC, a typical LCST effect in the polymeric matrix XU31591 wasobserved at a concentration of 23 wt %, while lower concentrations (1and 5 wt %) did not result in such temperature related behavior. Incontrast, PNIPAAM showed at all tested concentrations a LCST effect, at1 wt %, 5 wt %, and 23 wt % in polymeric matrix XU31591.

The lowest water vapor permeability values at high temperature (60° C.)was observed with Latex XU31904 at a coating thickness of 140 μm. Thiscombination also had the strongest decrease in water vapor permeabilitywith increasing temperature (20° C. to 60° C.). See FIG. 5.

The use of Lipacryl MB-304 resulted in a decrease of the activity of thetested LCST polymers compared to XU31591 and XU31904. PNIPAAM onlyshowed a LCST effect at 20 wt % in the coating, but not at a lowerconcentration of 5 wt %, while HPC did not show a LCST behavior at anyof tested concentrations (5 and 20 wt %) in Lipacryl MB-304.

For all three tested matrix polymers combined with HPC or PNIPAAM, LCSTbehavior was only observed at 75% RH, and not at 25% RH.

The results demonstrate that a desired thermoresponsive behavior of aLCST polymer in a polymeric matrix depends on several factors, such asthe amount of LCST in the coating, the type of the polymeric matrix inwhich the LCST polymer is distributed, the thickness of the coatings,and the relative humidity.

TABLE 5 Dry coating Permeability [US Perm] LCST Latex Thickness 25% RH75% RH Exp. LCST [wt %] [wt %] Latex [μm] 20° C. 60° C. 20° C. 60° C. E6HPC 1 99 Latex 82 2.5 2.6 3.3 3.5 XU31591 E7 PNIPAAM 1 99 Latex 82 3.33.2 8.0 5.3 XU31591 E8 HPC 5 95 Latex 78 2.0 3.5 2.8 3.6 XU31591 E9PNIPAAM 5 95 Latex 78 4.0 6.5 8.6 6.9 XU31591 E10 HPC 23 77 Latex 70 4.45.6 23.1 10.3 XU31591 E11 PNIPAAM 23 77 Latex 70 5.7 5.9 14.3 10.6XU31591 E12 HPC 23 77 Latex 140 0.85 1.4 23 5.8 XU31904 E13 PNIPAAM 2377 Latex 140 1.1 1.6 15.2 2.8 XU31904 E14 HPC 5 95 Lipacryl 73 7.9 8.89.9 14.9 MB-3041 E15 PNIPAAM 5 95 Lipacryl 73 7.4 9.1 11.5 14.4 MB-304E16 HPC 20 80 Lipacryl 67 8.8 9.8 18.9 18.9 MB-304 E17 PNIPAAM 20 80Lipacryl 67 20.9 16.1 39.2 34.0 MB-304 E18 0 100 Latex 77 4.7 4.3 8.58.6 XU31591 E19 100 Latex 77 0.7 1.4 1.9 3.6 XU31904 E20 0 100 Lipacryl74 8.2 8.5 8.3 9.3 MB-304

Example 5

LCST Polymer Grafted on Cross-Linked Polyurethane

A liquid coating composition was prepared mixing together at roomtemperature 50 wt % ethyl acetate (solvent), 2.5 wt % ethylene glycol;31.5 wt % Desmodur N75MPA (an isocyanate from Covestro), and 16 wt %Jeffamine M2005™-brand LCST polymer. Coated paper samples have beenprepared according to the same procedure as described in Example 2. Thewater vapor permeability was measured for the dried samples at 75% RHand varying temperatures in a range from 20° C. to 50° C. It can be seenin Table 6 that the water vapor permeability decreased with increasingtemperatures in the tested range of 20° C. to 40° C., and appeared toreach a plateau at 40° C. Not to be bound by theory, the resultsindicate that also if the LCST polymer is chemically bound to a matrixpolymer (in the present example to a polyurethane), the LCST polymer canprovide a LCST effect, i.e., decreasing the water vapor permeabilitywith increasing temperature.

TABLE 6 Thickness LCST LCST in of dry Polymer/ dry coating coatingPermeability [US Perm] Sample Matrix [wt %] [μm] 10° C. 20° C. 30° C.40° C. 50° C. E1 Jeffamine ™/ 10 100 28.5 14.6 10.0 10.3 grafted onPolyurethane

Measurement of the Water Vapor Permeability at Different Temperaturesand Different Humidities

The water vapor permeability at 25% RH and 75% RH of all coated papersamples have been measured according to ASTM E96 (2014), also called thecup test method.

The testing chamber was first set to 20° C. and 50% RH. This allowed themeasurement of water vapor permeability values below the LCST at both25% RH and 75% RH based on the dry and wet cup, respectively. Datapoints (cup weights) were measured every 1-2 hours. Because saturationof the dry cups may occur within 24 hours, at least six data points hadto be taken within the 24 hour time frame. Once enough data points at20° C. were obtained, the chamber was set to 60° C. and 50% RH. Thisallowed the determination of permeability values above the LCST at both25% RH and 75% RH. At the higher temperature, data points were takenevery 30-45 minutes, because saturation of the dry cups may occur within5-6 hours, and at least six data points should be taken within this timeframe.

All measured permeability values are average values of two independentcoating samples.

In the foregoing specification, the concepts have been described withreference to specific embodiments. However, one of ordinary skill in theart appreciates that various modifications and changes can be madewithout departing from the scope of the invention as set forth in theclaims below. Accordingly, the specification and figures are to beregarded in an illustrative rather than a restrictive sense, and allsuch modifications are intended to be included within the scope of theinvention.

What is claimed is:
 1. A building assembly comprising a buildingsubstrate and a weather resistive barrier (WRB), the WRB having a watervapor permeability that decreases with increasing temperature in atemperature range from 5° C. to 60° C. at 25% relative humidity (RH). 2.The building assembly of claim 1, wherein the WRB comprises a coatingincluding a lower critical solution temperature (LCST) polymer.
 3. Thebuilding assembly of claim 2, wherein the coating further comprises asecond polymer different from the LCST polymer.
 4. The building assemblyof claim 2, wherein the LCST polymer includes a hydroxyalkyl cellulose,a poly(alkylacrylamide), a poly(vinyl methyl ether), a polyetheramine,or any combination thereof.
 5. The building assembly of claim 4, whereinthe LCST polymer includes a hydroxypropylcellulose,Poly(N-isopropylacrylamide), poly(N-(tert-butyl)acrylamide), a monoamineof a poly(ethylene propylene) copolymer, or any combination thereof. 6.The building assembly of claim 2, wherein an amount of the LCST polymerin the coating is at least 0.5 wt % based on the total weight of thecoating.
 7. The building assembly of claim 3, wherein the second polymerincludes an acrylic polymer, an acrylic copolymer, a styrene acryliccopolymer, a vinyl acetate polymer, a vinyl acetate ethylene copolymer,an olefin wax, a polyethylene, a polypropylene, a polyurethane, apolyester, a vinylidene chloride polymer, a butadiene-vinylidenechloride copolymer, a styrene-butadiene copolymer, anacrylonitrile-butadiene copolymer, or any combination thereof.
 8. Thebuilding assembly of claim 2, wherein the WRB further comprises at leastone of an UV absorber, a filler, a dye, an anti-foaming agent, aviscosity modifier, a dispersant, a surfactant, or any combinationthereof.
 9. The building assembly of claim 2, wherein the coating of theWRB has a thickness of at least 10 μm and not greater than 500 μm. 10.The building assembly of claim 1, wherein the water vapor permeabilityof the WRB has a decrease of at least 50% at a temperature increase from5° C. to 60° C.
 11. The building assembly of claim 1, wherein the watervapor permeability of the WRB at a temperature of 25° C. or below is atleast 12 US perms, and a water vapor permeability at a temperature of45° C. or greater is not greater than 6 US perms.
 12. The buildingassembly of claim 2, wherein the coating is a one-layer-coating and thecoating is in direct contact with at least one outer surface of thebuilding substrate.
 13. The building assembly of claim 12, wherein thebuilding substrate is a board, a panel, or a siding.
 14. The buildingassembly of claim 13, wherein the building substrate is a boardcomprising gypsum.
 15. A sheet for use as a WRB comprising a coating,wherein the coating comprises a LCST polymer and a second polymer; thesheet has an air permeability of less than 0.02 L/(s m²) at a pressureof 75 Pa; and a water vapor permeability of the sheet decreases withincreasing temperature in a temperature range from 5° C. to 60° C. 16.The sheet of claim 15, wherein the sheet comprises a porous substrate,and the coating overlies a first surface of the porous substrate. 17.The sheet of claim 15, wherein the water vapor permeability of the sheethas a decrease of at least 50% at a temperature increase from 5° C. to60° C.
 18. The sheet of claim 15, wherein the sheet further comprises anadhesive layer and is a self-adhered sheet.
 19. The sheet of claim 15,wherein the second polymer includes an acrylic polymer, an acryliccopolymer, a styrene acrylic copolymer, a vinyl acetate polymer, a vinylacetate ethylene copolymer, an olefin wax, a polyethylene, apolypropylene, a polyurethane, a polyester, a vinylidene chloridepolymer, a butadiene-vinylidene chloride copolymer, a styrene-butadienecopolymer, an acrylonitrile-butadiene copolymer, or any combinationthereof.
 20. The sheet of claim 15, wherein the LCST polymer includesPoly(N-isopropylacrylamide) and the second polymer includesbutadiene-vinylidene chloride.
 21. A liquid coating compositioncomprising at least one LCST polymer and at least one second polymer,wherein a solid coating formed by the liquid coating composition has anair permeability of less than 0.02 L/(s m²) at a pressure of 75 Pa; anda water vapor permeability of the solid coating decreases withincreasing temperature in a temperature range from 5° C. to 60° C. 22.The liquid coating composition of claim 21, wherein the LCST polymerincludes a hydroxyalkyl cellulose, a poly(alkylacrylamide), a poly(vinylmethyl ether), a polyetheramine, or any combination thereof.
 23. Theliquid coating composition of claim 21, wherein the second polymerincludes an acrylic polymer, an acrylic copolymer, a styrene acryliccopolymer, a vinyl acetate polymer, a vinyl acetate ethylene copolymer,an olefin wax, a polyethylene, a polypropylene, a polyurethane, apolyester, a vinylidene chloride polymer, a butadiene-vinylidenechloride copolymer, a styrene-butadiene copolymer, anacrylonitrile-butadiene copolymer, or any combination thereof.
 24. Theliquid coating composition of claim 21, wherein the LCST polymerincludes Poly(N-isopropylacrylamide) and the second polymer includesbutadiene-vinylidene chloride.